NDC 51662-1544
Naloxone Hydrochloride 0.4 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from AuroMedics Pharma LLC's NDC 55150-327.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Naloxone: every company that makes it
- Form
- injection, solution, intramuscular; intravenous; subcutaneous
- Strength
- 0.4 mg per 1 mL
- Approval
- ANDA ANDA212455
- On the market since
- Aug 8, 2021
- Package NDCs
51662-1544-151662-1544-251662-1544-3- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2024
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